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Inhibitory effect of amidino-substituted heterocyclic compounds on the amidase activity of plasmin and of high and low molecular weight urokinase and on urokinase-induced plasminogen activation.

作者信息

Geratz J D, Shaver S R, Tidwell R R

出版信息

Thromb Res. 1981;24(1-2):73-83. doi: 10.1016/0049-3848(81)90033-5.

DOI:10.1016/0049-3848(81)90033-5
PMID:6460342
Abstract
摘要

相似文献

1
Inhibitory effect of amidino-substituted heterocyclic compounds on the amidase activity of plasmin and of high and low molecular weight urokinase and on urokinase-induced plasminogen activation.脒基取代杂环化合物对纤溶酶、高分子量及低分子量尿激酶的酰胺酶活性以及对尿激酶诱导的纤溶酶原激活的抑制作用。
Thromb Res. 1981;24(1-2):73-83. doi: 10.1016/0049-3848(81)90033-5.
2
Kinetic study of the effect of heparin on the amidase activity of trypsin, plasmin and urokinase.肝素对胰蛋白酶、纤溶酶和尿激酶酰胺酶活性影响的动力学研究。
Thromb Haemost. 1983 Jun 28;49(3):199-203.
3
Covalent molecular weight approximately 92 000 hybrid plasminogen activator derived from human plasmin amino-terminal and urokinase carboxyl-terminal domains.共价分子量约为92000的杂合型纤溶酶原激活剂，其来源于人纤溶酶氨基末端和尿激酶羧基末端结构域。
Biochemistry. 1986 Jun 17;25(12):3603-11. doi: 10.1021/bi00360a019.
4
Differences in the reactivities of human urokinase and the porcine tissue plasminogen activator.
Haemostasis. 1976;5(5):295-305. doi: 10.1159/000214148.
5
Plasmin and plasminogen activators: kinetics, and kinetics of plasminogen activation.纤溶酶和纤溶酶原激活剂：动力学以及纤溶酶原激活的动力学
Ann N Y Acad Sci. 1981;370:588-91. doi: 10.1111/j.1749-6632.1981.tb29765.x.
6
Stimulation of plasmin catalyzed conversion of single-chain to two-chain urokinase-type plasminogen activator by sulfated polysaccharides.
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7
Activation of human neo-plasminogen-Val442 by urokinase and streptokinase and a kinetic characterization of neoplasmin-Val442.尿激酶和链激酶对人新型纤溶酶原-Val442的激活作用以及新型纤溶酶-Val442的动力学特征
J Biol Chem. 1980 Jun 10;255(11):5329-35.
8
Activation pathway of glu-plasminogen to Lys-plasmin by urokinase.尿激酶将谷氨酰胺-纤溶酶原激活为赖氨酸-纤溶酶的途径。
Thromb Res. 1982 Sep 15;27(6):671-7. doi: 10.1016/0049-3848(82)90005-6.
9
Conversion of Glu-plasminogen to plasmin by urokinase in the presence of tranexamic acid.在氨甲环酸存在的情况下，尿激酶将谷氨酸纤溶酶原转化为纤溶酶。
Thromb Res. 1981 May 15;22(4):437-43. doi: 10.1016/0049-3848(81)90105-5.
10
Monoclonal antibodies inhibitory to human plasmin. Definitive demonstration of a role for plasmin in activating the proenzyme of urokinase-type plasminogen activator.
Eur J Biochem. 1986 Aug 1;158(3):537-42. doi: 10.1111/j.1432-1033.1986.tb09787.x.

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Antimicrob Agents Chemother. 1998 Mar;42(3):666-74. doi: 10.1128/AAC.42.3.666.
2
Enhancement of respiratory syncytial virus-induced cytopathology by trypsin, thrombin, and plasmin.胰蛋白酶、凝血酶和纤溶酶增强呼吸道合胞病毒诱导的细胞病变效应
Infect Immun. 1983 Apr;40(1):351-8. doi: 10.1128/iai.40.1.351-358.1983.
3
In vitro inhibition of human sarcoma cells' invasive ability by bis(5-amidino-2-benzimidazolyl)methane--a novel esteroprotease inhibitor.
双（5-脒基-2-苯并咪唑基）甲烷——一种新型酯蛋白酶抑制剂对人肉瘤细胞侵袭能力的体外抑制作用
Am J Pathol. 1986 Apr;123(1):46-56.
4
Amelioration of immune complex-mediated glomerulonephritis by synthetic protease inhibitors.合成蛋白酶抑制剂对免疫复合物介导的肾小球肾炎的改善作用
Am J Pathol. 1987 Jun;127(3):499-506.
5
Sequential events in the pathogenesis of streptococcal cell wall-induced arthritis and their modulation by bis(5-amidino-2-benzimidazolyl)methane (BABIM).链球菌细胞壁诱导性关节炎发病机制中的连续事件及其被双（5-脒基-2-苯并咪唑基）甲烷（BABIM）的调节
Am J Pathol. 1990 Apr;136(4):909-21.
6
Streptococcal cell wall-induced systemic disease. Beneficial effects of trans-bis(5-amidino-2-benzimidazolyl)ethene, a novel, macrophage-directed anti-inflammatory agent.链球菌细胞壁诱导的全身性疾病。新型巨噬细胞导向抗炎剂反式双（5-脒基-2-苯并咪唑基）乙烯的有益作用。
Am J Pathol. 1991 Oct;139(4):921-31.